Work Flexibility: HybridPosition SummaryThe Senior Staff Engineer will drive a culture of automation, innovation, and continuous improvement to support the Neurovascular product portfolio. The engineer will have a deep technical expertise, be a strategic thinking, and have strong leadership capabilities to develop and implement solutions that enhance our operational efficiency and product quality.The Engineer will work closely with cross-functional teams—including Manufacturing, R&D, Quality, and Regulatory Affairs—to deliver reliable, validated automation solutions that support scalability and compliance.This position requires both hands-on technical expertise and strong project management skills to bring innovative automation solutions from concept to production within a highly regulated environment.Key Areas of ResponsibilityOversee automation projects from conception to execution, ensuring alignment with organizational goals.Contribute and input into Engineering functional strategy.Collaborate with cross-functional teams to identify automation opportunities and prioritize initiatives.Be a Technological expert, willing to source, investigate and implement technological and automation advances.Lead design, development, testing & refinement of automated system, sub-system & component.Process validation for products and processes; VP, IQ, OQ, PQ and associated documentation.Observing the Quality Management Systems requirements on site at all timesSupport the implementation of automation strategies across projects.Technical leadership of Staff engineers, Senior engineers, Engineers, Coop students, and Technicians.Co-ordinates with other unit’s vendors and senior managers as needed to ensure specific cost, time, and regulatory standards achieved.Communicates with business partners to resolve process and product issues.Champion operations excellence across the siteAdherence to, and enforcement of all Environment Health and Safety (EHS) requirements on site.Qualifications / Knowledge / SkillsLevel 8 Degree or Masters in relevant Engineering or Science discipline (Manufacturing, Mechanical, etc) or technical experience equivalency.Minimum of 6 years’ experience.Recognised Lean qualification, ideally a black belt.Experience with medical device manufacturing processes (e.g., cleanroom automation, micro-assembly, automated testing).Technological expert, willing to source, investigate and implement technological and automation advances.Proven Project Management skills through the delivery of business-critical projects.Confident and effective decision maker, with a proven technical leadership ability to negotiate and influence others.Effective technical documentation and change control in regulated environments.Excellent cross-functional collaboration with Manufacturing, Quality, and R&D teams.Capable of technically leading a multi-disciplined team in a dynamic, regulated and results motivated environment.Demonstrable Excellent analytical & critical thinking skills, a process improvement orientation.Demonstrable ability to lead significant projects and initiatives.Familiarity with GAMP 5 and computer system validation (CSV) for automated equipment.Understanding of ISO 13485, ISO 14971, and FDA 21 CFR Part 11 compliance in automation systems.Experience with integration of MES/ERP systems for manufacturing data traceability.Proficient in CAD tools for fixture and tooling design (SolidWorks or similar).#IJTravel Percentage: 10%
